Loratadineantihistamine description, usages, side effects, indications, overdosage, supplying and lots more!

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Loratadineantihistamine

REMEDYREPACK INC.

Perrigo Loratadine Tablets, 10 mg Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

OTC - ACTIVE INGREDIENT

Loratadine 10 mg

 

OTC - PURPOSE

Antihistamine

 

INDICATIONS & USAGE

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

  • runny nose
  • sneezing
  • itchy, watery eyes
  • itching of the nose or throat

 

WARNINGS

if you have ever had an allergic reaction to this product or any of its ingredients

 

liver or kidney disease. Your doctor should determine if you need a different dose.

 

do not take more than directed. Taking more than directed may cause drowsiness.

 

an allergic reaction to this product occurs. Seek medical help right away.

 

ask a health professional before use.

 

In case of overdose, get medical help or contact a Poison Control Center right away.

 

DOSAGE & ADMINISTRATION

adults and children 6 years and over 1 tablet daily; not more than 1 tablet in 24 hours
children under 6 years of age ask a doctor
consumers with liver or kidney disease ask a doctor

 

STORAGE AND HANDLING

  • do not use if printed foil under cap is broken or missing
  • store at 20°-25°C (68°-77°F)

 

INACTIVE INGREDIENT

lactose monohydrate, magnesium stearate, povidone, pregelatinized starch

 

OTC - QUESTIONS

1-800-719-9260

 

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION

DRUG: Loratadineantihistamine antihistamine


GENERIC: Loratadine


DOSAGE: TABLET


ADMINSTRATION: ORAL


NDC: 52125-600-08


ACTIVE INGREDIENT(S):

  • LORATADINE 10mg in 1


INACTIVE INGREDIENT(S):

  • LACTOSE MONOHYDRATE
  • POVIDONE
  • MAGNESIUM STEARATE
  • STARCH, CORN


COLOR: white


SHAPE: OVAL


SCORE: No score


SIZE: 8 mm


IMPRINT: L612


PACKAGING: 10 in 1 VIAL



Loratadineantihistamine

Loratadineantihistamine

Loratadineantihistamine

Loratadine TABLET

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:52125-600(NDC:45802-650)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
LORATADINE loratadine 10 mg

Inactive Ingredients

Ingredient Name Strength
lactose monohydrate
povidone
MAGNESIUM STEARATE
STARCH, CORN

Product Characteristics

Color Size Imprint Code Shape
white 8 mm L612 OVAL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:52125-600-08 10 in 1 VIAL

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076301 2013-05-28


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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